Quality Control Technician / Microbiologist

Aequor; Athens (GA); On-site; USD 52,000 - 68,000; Full time

Job summary

Boehringer Ingelheim is seeking a Quality Control Technician III to support bioanalytical testing within the Quality Control department. The role involves executing validated testing methods, maintaining documentation, and ensuring GMP compliance in a fast-paced lab environment.

The ideal candidate will perform a range of bioanalytical assays on materials and samples, follow approved procedures, and contribute to a culture of quality and safety across the site.

Qualifications

• Aseptic technique knowledge and hands-on experience.
• Experience with laboratory-based testing in regulated environments.
• Ability to follow detailed testing procedures and documentation.
• Strong attention to detail and commitment to quality.
• Effective written and verbal communication skills.

Responsibilities

• Perform bioanalytical testing using validated methods.
• Conduct quality control assays including immunological, microbiological, molecular, and virological tests.
• Test raw materials, in-process materials, release samples, and stability samples.
• Initiate, execute, document, and complete laboratory assays per procedures and timelines.
• Ensure compliance with 9 CFR, EU regulatory requirements, VICH guidelines, GMP standards and company procedures.
• Maintain accurate laboratory documentation and communicate status to supervisors promptly.
• Support site safety initiatives and adhere to safety KPIs.

Skills

Aseptic technique

Regulated environment testing

Follow procedures

Attention to detail

Written and verbal communication

Education

Degree requirements not specified by the client

Job description

Position Summary

Boehringer Ingelheim is seeking a Quality Control Technician III to support bioanalytical testing activities within the Quality Control department. This role is responsible for performing a variety of Bio-QC assays on raw materials, in-process samples, release testing samples, and stability samples while ensuring compliance with regulatory and Good Manufacturing Practice (GMP) requirements.

The successful candidate will execute validated testing methods, maintain accurate documentation, ensure compliance with quality standards, and contribute to a safe and efficient laboratory environment.

Key Responsibilities

• Perform bioanalytical testing using validated methods and procedures.


• Conduct quality control assays including:


• Immunological testing


• Microbiological testing


• Molecular biological assays


• Virological assays


• Test raw materials, in-process materials, release samples, and stability samples.


• Initiate, execute, document, and complete laboratory assays according to approved procedures and timelines.


• Ensure compliance with:


• 9 CFR regulations


• European Union (EU) regulatory requirements


• VICH guidelines


• GMP standards


• Company quality and compliance procedures


• Maintain accurate and complete laboratory documentation.


• Communicate testing status, scheduling concerns, deviations, and compliance issues to supervisors in a timely manner.


• Support site safety initiatives and adhere to established safety KPIs.


• Follow production outlines, special testing protocols, and quality standards.


• Demonstrate company leadership principles and contribute to a culture of quality and compliance.

Required Qualifications

Skills & Experience

• Strong knowledge and practical experience with aseptic technique.


• Experience performing laboratory-based testing in a regulated environment.


• Ability to follow detailed testing procedures and documentation requirements.


• Strong attention to detail and commitment to quality standards.


• Effective written and verbal communication skills.

Education

• Degree requirements not specified by the client.


• Language Requirements


• Reading


• Writing


• Speaking

Preferred Qualifications

Experience with microbiological testing.

Previous experience working in a GMP-regulated manufacturing or laboratory environment.

Familiarity with pharmaceutical, biologics, biotechnology, or animal health quality control testing operations.

• Laboratory-based quality control environment.


• Strict adherence to aseptic practices, safety protocols, and GMP documentation standards.


• Requires handling biological materials and working within regulated testing environments.


• Collaboration with Quality Control, Manufacturing, and Compliance teams.